Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells
- Autores
- Pérez, G.; Pregi, N.; Vittori, D.; Di Risio, C.; Garbossa, G.; Nesse, A.
- Año de publicación
- 2005
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Aluminum (Al) and iron (Fe) share several physicochemical characteristics and they both bind to transferrin (Tf), entering the cell via Tf receptors (TfR). Previously, we found similar values of affinity constant for the binding of TfR to Tf carrying either Al or Fe. The competitive interaction between both metals prevented normal Fe incorporation into K562 cells and triggered the upregulation of Fe transport. In the present work we demonstrated that Al modified Fe uptake without affecting the expression of Tf receptors. Both TfR and TfR2 mRNA levels, evaluated by RT-PCR, and TfR antigenic sites, analyzed by flow cytometry, were found unchanged after Al exposure. In turn, Al did induce upregulation of non-Tf bound Fe (NTBI) uptake. This modulation was not due to intracellular Fe decrease since NTBI transport proved not to be regulated by Fe depletion. Unlike its behavior in the presence of Tf, Al was unable to compete with NTBI uptake, suggesting that both metals do not share the same alternative transport pathway. We propose that Al interference with TfR-mediated Fe incorporation might trigger the upregulation of NTBI uptake, an adaptation aimed at incorporating the essential metal required for cellular metabolism without allowing the simultaneous access of a potentially toxic metal. © 2004 Elsevier B.V. All rights reserved.
Fil:Pérez, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Pregi, N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Vittori, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Di Risio, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Garbossa, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fil:Nesse, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. - Fuente
- Biochim. Biophys. Acta Mol. Cell Res. 2005;1745(1):124-130
- Materia
-
Aluminum
Iron metabolism
K562 cell line
Non-transferrin bound iron transport
Transferrin receptor
Transferrin-mediated iron uptake
aluminum
antigen
iron
messenger RNA
receptor subtype
transferrin
transferrin receptor
article
chronic myeloid leukemia
controlled study
flow cytometry
human
human cell
iron depletion
iron transport
leukemia cell
priority journal
protein expression
receptor binding
regulatory mechanism
reverse transcription polymerase chain reaction
upregulation
Aluminum
Biological Transport
Butyrates
Cell Differentiation
Gene Expression Regulation, Neoplastic
Humans
Iron
K562 Cells
Receptors, Transferrin
RNA, Messenger
Transferrin - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/2.5/ar
- Repositorio
- Institución
- Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
- OAI Identificador
- paperaa:paper_01674889_v1745_n1_p124_Perez
Ver los metadatos del registro completo
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Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cellsPérez, G.Pregi, N.Vittori, D.Di Risio, C.Garbossa, G.Nesse, A.AluminumIron metabolismK562 cell lineNon-transferrin bound iron transportTransferrin receptorTransferrin-mediated iron uptakealuminumantigenironmessenger RNAreceptor subtypetransferrintransferrin receptorarticlechronic myeloid leukemiacontrolled studyflow cytometryhumanhuman celliron depletioniron transportleukemia cellpriority journalprotein expressionreceptor bindingregulatory mechanismreverse transcription polymerase chain reactionupregulationAluminumBiological TransportButyratesCell DifferentiationGene Expression Regulation, NeoplasticHumansIronK562 CellsReceptors, TransferrinRNA, MessengerTransferrinAluminum (Al) and iron (Fe) share several physicochemical characteristics and they both bind to transferrin (Tf), entering the cell via Tf receptors (TfR). Previously, we found similar values of affinity constant for the binding of TfR to Tf carrying either Al or Fe. The competitive interaction between both metals prevented normal Fe incorporation into K562 cells and triggered the upregulation of Fe transport. In the present work we demonstrated that Al modified Fe uptake without affecting the expression of Tf receptors. Both TfR and TfR2 mRNA levels, evaluated by RT-PCR, and TfR antigenic sites, analyzed by flow cytometry, were found unchanged after Al exposure. In turn, Al did induce upregulation of non-Tf bound Fe (NTBI) uptake. This modulation was not due to intracellular Fe decrease since NTBI transport proved not to be regulated by Fe depletion. Unlike its behavior in the presence of Tf, Al was unable to compete with NTBI uptake, suggesting that both metals do not share the same alternative transport pathway. We propose that Al interference with TfR-mediated Fe incorporation might trigger the upregulation of NTBI uptake, an adaptation aimed at incorporating the essential metal required for cellular metabolism without allowing the simultaneous access of a potentially toxic metal. © 2004 Elsevier B.V. All rights reserved.Fil:Pérez, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Pregi, N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Vittori, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Di Risio, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Garbossa, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.Fil:Nesse, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.2005info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_01674889_v1745_n1_p124_PerezBiochim. Biophys. Acta Mol. Cell Res. 2005;1745(1):124-130reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-09-29T13:43:05Zpaperaa:paper_01674889_v1745_n1_p124_PerezInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-09-29 13:43:06.953Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse |
dc.title.none.fl_str_mv |
Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells |
title |
Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells |
spellingShingle |
Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells Pérez, G. Aluminum Iron metabolism K562 cell line Non-transferrin bound iron transport Transferrin receptor Transferrin-mediated iron uptake aluminum antigen iron messenger RNA receptor subtype transferrin transferrin receptor article chronic myeloid leukemia controlled study flow cytometry human human cell iron depletion iron transport leukemia cell priority journal protein expression receptor binding regulatory mechanism reverse transcription polymerase chain reaction upregulation Aluminum Biological Transport Butyrates Cell Differentiation Gene Expression Regulation, Neoplastic Humans Iron K562 Cells Receptors, Transferrin RNA, Messenger Transferrin |
title_short |
Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells |
title_full |
Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells |
title_fullStr |
Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells |
title_full_unstemmed |
Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells |
title_sort |
Aluminum exposure affects transferrin-dependent and -independent iron uptake by K562 cells |
dc.creator.none.fl_str_mv |
Pérez, G. Pregi, N. Vittori, D. Di Risio, C. Garbossa, G. Nesse, A. |
author |
Pérez, G. |
author_facet |
Pérez, G. Pregi, N. Vittori, D. Di Risio, C. Garbossa, G. Nesse, A. |
author_role |
author |
author2 |
Pregi, N. Vittori, D. Di Risio, C. Garbossa, G. Nesse, A. |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Aluminum Iron metabolism K562 cell line Non-transferrin bound iron transport Transferrin receptor Transferrin-mediated iron uptake aluminum antigen iron messenger RNA receptor subtype transferrin transferrin receptor article chronic myeloid leukemia controlled study flow cytometry human human cell iron depletion iron transport leukemia cell priority journal protein expression receptor binding regulatory mechanism reverse transcription polymerase chain reaction upregulation Aluminum Biological Transport Butyrates Cell Differentiation Gene Expression Regulation, Neoplastic Humans Iron K562 Cells Receptors, Transferrin RNA, Messenger Transferrin |
topic |
Aluminum Iron metabolism K562 cell line Non-transferrin bound iron transport Transferrin receptor Transferrin-mediated iron uptake aluminum antigen iron messenger RNA receptor subtype transferrin transferrin receptor article chronic myeloid leukemia controlled study flow cytometry human human cell iron depletion iron transport leukemia cell priority journal protein expression receptor binding regulatory mechanism reverse transcription polymerase chain reaction upregulation Aluminum Biological Transport Butyrates Cell Differentiation Gene Expression Regulation, Neoplastic Humans Iron K562 Cells Receptors, Transferrin RNA, Messenger Transferrin |
dc.description.none.fl_txt_mv |
Aluminum (Al) and iron (Fe) share several physicochemical characteristics and they both bind to transferrin (Tf), entering the cell via Tf receptors (TfR). Previously, we found similar values of affinity constant for the binding of TfR to Tf carrying either Al or Fe. The competitive interaction between both metals prevented normal Fe incorporation into K562 cells and triggered the upregulation of Fe transport. In the present work we demonstrated that Al modified Fe uptake without affecting the expression of Tf receptors. Both TfR and TfR2 mRNA levels, evaluated by RT-PCR, and TfR antigenic sites, analyzed by flow cytometry, were found unchanged after Al exposure. In turn, Al did induce upregulation of non-Tf bound Fe (NTBI) uptake. This modulation was not due to intracellular Fe decrease since NTBI transport proved not to be regulated by Fe depletion. Unlike its behavior in the presence of Tf, Al was unable to compete with NTBI uptake, suggesting that both metals do not share the same alternative transport pathway. We propose that Al interference with TfR-mediated Fe incorporation might trigger the upregulation of NTBI uptake, an adaptation aimed at incorporating the essential metal required for cellular metabolism without allowing the simultaneous access of a potentially toxic metal. © 2004 Elsevier B.V. All rights reserved. Fil:Pérez, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Pregi, N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Vittori, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Di Risio, C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Garbossa, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Nesse, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. |
description |
Aluminum (Al) and iron (Fe) share several physicochemical characteristics and they both bind to transferrin (Tf), entering the cell via Tf receptors (TfR). Previously, we found similar values of affinity constant for the binding of TfR to Tf carrying either Al or Fe. The competitive interaction between both metals prevented normal Fe incorporation into K562 cells and triggered the upregulation of Fe transport. In the present work we demonstrated that Al modified Fe uptake without affecting the expression of Tf receptors. Both TfR and TfR2 mRNA levels, evaluated by RT-PCR, and TfR antigenic sites, analyzed by flow cytometry, were found unchanged after Al exposure. In turn, Al did induce upregulation of non-Tf bound Fe (NTBI) uptake. This modulation was not due to intracellular Fe decrease since NTBI transport proved not to be regulated by Fe depletion. Unlike its behavior in the presence of Tf, Al was unable to compete with NTBI uptake, suggesting that both metals do not share the same alternative transport pathway. We propose that Al interference with TfR-mediated Fe incorporation might trigger the upregulation of NTBI uptake, an adaptation aimed at incorporating the essential metal required for cellular metabolism without allowing the simultaneous access of a potentially toxic metal. © 2004 Elsevier B.V. All rights reserved. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/20.500.12110/paper_01674889_v1745_n1_p124_Perez |
url |
http://hdl.handle.net/20.500.12110/paper_01674889_v1745_n1_p124_Perez |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/2.5/ar |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
Biochim. Biophys. Acta Mol. Cell Res. 2005;1745(1):124-130 reponame:Biblioteca Digital (UBA-FCEN) instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales instacron:UBA-FCEN |
reponame_str |
Biblioteca Digital (UBA-FCEN) |
collection |
Biblioteca Digital (UBA-FCEN) |
instname_str |
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
instacron_str |
UBA-FCEN |
institution |
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repository.name.fl_str_mv |
Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
repository.mail.fl_str_mv |
ana@bl.fcen.uba.ar |
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